CAP BUNDLE KIT DYNDC2137
Class I - Dangerous 🏥 Medical Devices
Recalled: April 24, 2019 Centurion Medical Products Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: 2018091390 2018120590
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Centurion Medical Products Corporation
- Reason for Recall:
- Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
CAP BUNDLE KIT DYNDC2137
Product Codes/Lot Numbers:
2018091390 2018120590
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0087-2020
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